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Anzahl der Publikationen: 5
Zeitschriftenartikel
Sommer, Anna K.; te Paske, Iris B. A. W.; Garcia-Pelaez, Jose; Laner, Andreas; Holinski-Feder, Elke; Steinke-Lange, Verena; Peters, Sophia; Valle, Laura; Spier, Isabel; Huntsman, David; de Voer, Richarda M.; Hoogerbrugge, Nicoline; Aretz, Stefan und Oliveira, Carla
(2022):
Solving the genetic aetiology of hereditary gastrointestinal tumour syndromes- a collaborative multicentre endeavour within the project Solve-RD.
In: European Journal of Medical Genetics, Bd. 65, Nr. 5, 104475
Moller, Pal; Seppala, Toni; Dowty, James G.; Haupt, Saskia; Dominguez-Valentin, Mev; Sunde, Lone; Bernstein, Inge; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capella, Gabriel; Evans, Dafydd Gareth; Burn, John; Holinski-Feder, Elke; Bertario, Lucio; Bonanni, Bernardo; Lindblom, Annika; Levi, Zohar; Macrae, Finlay; Winship, Ingrid; Plazzer, John-Paul; Sijmons, Rolf; Laghi, Luigi; Della Valle, Adriana; Heinimann, Karl; Half, Elizabeth; Lopez-Koestner, Francisco; Alvarez-Valenzuela, Karin; Scott, Rodney J.; Katz, Lior; Laish, Ido; Vainer, Elez; Vaccaro, Carlos Alberto; Carraro, Dirce Maria; Gluck, Nathan; Abu-Freha, Naim; Stakelum, Aine; Kennelly, Rory; Winter, Des; Rossi, Benedito Mauro; Greenblatt, Marc; Bohorquez, Mabel; Sheth, Harsh; Tibiletti, Maria Grazia; Lino-Silva, Leonardo S.; Horisberger, Karoline; Portenkirchner, Carmen; Nascimento, Ivana; Rossi, Norma Teresa; da Silva, Leandro Apolinario; Thomas, Huw; Zarand, Attila; Mecklin, Jukka-Pekka; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Peltomaki, Paivi; Therkildsen, Christina; Lindberg, Lars Joachim; Thorlacius-Ussing, Ole; Knebel Doeberitz, Magnus von; Loeffler, Markus; Rahner, Nils; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Hueneburg, Robert; de Vargas, Aida Falcon; Latchford, Andrew; Gerdes, Anne-Marie; Backman, Ann-Sofie; Guillen-Ponce, Carmen; Snyder, Carrie; Lautrup, Charlotte K.; Amor, David; Palmero, Edenir; Stoffel, Elena; Duijkers, Floor; Hall, Michael J.; Hampel, Heather; Williams, Heinric; Okkels, Henrik; Lubinski, Jan; Reece, Jeanette; Ngeow, Joanne; Guillem, Jose G.; Arnold, Julie; Wadt, Karin; Monahan, Kevin; Senter, Leigha; Rasmussen, Lene J.; Hest, Liselotte P. van; Ricciardiello, Luigi; Kohonen-Corish, Maija R. J.; Ligtenberg, Marjolijn J. L.; Southey, Melissa; Aronson, Melyssa; Zahary, Mohd N.; Samadder, N. Jewel; Poplawski, Nicola; Hoogerbrugge, Nicoline; Morrison, Patrick J.; James, Paul; Lee, Grant; Chen-Shtoyerman, Rakefet; Ankathil, Ravindran; Pai, Rish; Ward, Robyn; Parry, Susan; Debniak, Tadeusz; John, Thomas; Overeem Hansen, Thomas van; Caldes, Trinidad; Yamaguchi, Tatsuro; Barca-Tierno, Veronica; Garre, Pilar; Cavestro, Giulia Martina; Weitz, Juergen; Redler, Silke; Buettner, Reinhard; Heuveline, VincentZ; Hopper, John L.; Win, Aung Ko; Lindor, Noralane; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane; Buchanan, Daniel D.; Thibodeau, Stephen N.; ten Broeke, Sanne W.; Hovig, Eivind; Nakken, Sigve; Pineda, Marta; Duenas, Nuria; Brunet, Joan; Green, Kate; Lalloo, Fiona; Newton, Katie; Crosbie, Emma J.; Mints, Miriam; Tjandra, Douglas; Neffa, Florencia; Esperon, Patricia; Kariv, Revital; Rosner, Guy; Pavicic, Walter Hernan; Kalfayan, Pablo; Torrezan, Giovana Tardin; Bassaneze, Thiago; Martin, Claudia; Moslein, Gabriela; Ahadova, Aysel; Kloor, Matthias; Sampson, Julian R. und Jenkins, Mark A.
(2022):
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
In: Hereditary Cancer in Clinical Practice, Bd. 20, Nr. 1, 36
Diets, Illja J.; van der Donk, Roos; Baltrunaite, Kristina; Waanders, Esme; Reijnders, Margot R. F.; Dingemans, Alexander J. M.; Pfundt, Rolph; Vulto-van Silfhout, Anneke T.; Wiel, Laurens; Gilissen, Christian; Thevenon, Julien; Perrin, Laurence; Afenjar, Alexandra; Nava, Caroline; Keren, Boris; Bartz, Sarah; Peri, Bethany; Beunders, Gea; Verbeek, Nienke; van Gassen, Koen; Thiffault, Isabelle; Cadieux-Dion, Maxime; Huerta-Saenz, Lina; Wagner, Matias; Konstantopoulou, Vassiliki; Vodopiutz, Julia; Griese, Matthias; Boel, Annekatrien; Callewaert, Bert; Brunner, Han G.; Kleefstra, Tjitske; Hoogerbrugge, Nicoline; de Vries, Bert B. A.; Hwa, Vivian; Dauber, Andrew; Hehir-Kwa, Jayne Y.; Kuiper, Roland P. und Jongmans, Marjolijn C. J.
(2019):
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism.
In: American Journal of Human Genetics, Bd. 104, Nr. 4: S. 758-766
Broeke, Sanne W. ten; Klift, Heleen M. van der; Tops, Carli M. J.; Aretz, Stefan; Bernstein, Inge; Buchanan, Daniel D.; Chapelle, Albert de la; Capella, Gabriel; Clendenning, Mark; Engel, Christoph; Gallinger, Steven; Gomez Garcia, Encarna; Figueiredo, Jane C.; Haile, Robert; Hampel, Heather L.; Hopper, John L.; Hoogerbrugge, Nicoline; Knebel Doeberitz, Magnus von; Le Marchand, Loic; Lettebör, Tom G. W.; Jenkins, Mark A.; Lindblom, Annika; Lindor, Noralane M.; Mensenkamp, Arjen R.; Moller, Pal; Newcomb, Polly A.; Os, Theo A. M. van; Pearlman, Rachel; Pineda, Marta; Rahner, Nils; Redeker, Egbert J. W.; Olderode-Berends, Maran J. W.; Rosty, Christophe; Schackert, Hans K.; Scott, Rodney; Senter, Leigha; Spruijt, Liesbeth; Steinke-Lange, Verena; Suerink, Manon; Thibodeau, Stephen; Vos, Yvonne J.; Wagner, Anja; Winship, Ingrid; Hes, Frederik J.; Vasen, Hans F. A.; Wijnen, Juul T.; Nielsen, Maartje und Win, Aung Ko
(2018):
Cancer Risks for PMS2-Associated Lynch Syndrome.
In: Journal of Clinical Oncology, Bd. 36, Nr. 29: S. 2961-2968
Vogelaar, Ingrid P.; Post, Rachel S. van der; Krieken, J. Han J. M. van; Spruijt, Liesbeth; Zelst-Stams, Wendy A. G. van; Kets, C. Marleen; Lubinski, Jan; Jakubowska, Anna; Teodorczyk, Urszula; Aalfs, Cora M.; Hest, Liselotte P. van; Pinheiro, Hugo; Oliveira, Carla; Jhangiani, Shalini N.; Muzny, Donna M.; Gibbs, Richard A.; Lupski, James R.; Ligt, Joep de; Vissers, Lisenka E. L. M.; Hoischen, Alexander; Gilissen, Christian; Vorst, Maartje van de; Goeman, Jelle J.; Schackert, Hans K.; Ranzani, Guglielmina N.; Molinaro, Valeria; Garcia, Encarna B. Gomez; Hes, Frederik J.; Holinski-Feder, Elke; Genuardi, Maurizio; Ausems, Margreet G. E. M.; Sijmons, Rolf H.; Wagner, Anja; Kolk, Lizet E. van der; Björnevoll, Inga; Hoberg-Vetti, Hildegunn; Kessel, Ad Geurts van; Kuiper, Roland P.; Ligtenberg, Marjolijn J. L. und Hoogerbrugge, Nicoline
(2017):
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing.
In: European Journal of Human Genetics, Bd. 25, Nr. 11: S. 1246-1252